rewirebio.iobenchmarks
Configuration

ESM-1b (Evo 2 paper variant effect evaluations)

Configuration of ESM-1b: Protein language model.

14 evaluations · 28 results

Overview

An explanatory profile has not yet been reviewed for this record.

Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

Evaluations and results

14 evaluations · 28 results. Different protocols are not a single leaderboard.

Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)

Sorted by AUPRC (zero-shot; ClinVar coding indels) (higher is better). The best value in each column is highlighted. Decimals are rounded for display; each value links to the printed value and its source.

Tested configurationProtocol and datasetAUPRC (zero-shot; ClinVar coding indels)AUPRC (zero-shot; ClinVar coding microsatellite variants)AUPRC (zero-shot; ClinVar coding non-SNVs, far from splice site)AUPRC (zero-shot; ClinVar coding non-SNVs, highly conserved)AUPRC (zero-shot; ClinVar coding non-SNVs, moderately conserved)AUPRC (zero-shot; ClinVar coding non-SNVs, not conserved)AUPRC (zero-shot; ClinVar coding non-SNVs, poorly conserved)AUPRC (zero-shot; ClinVar coding SNVs, far from splice site)AUPRC (zero-shot; ClinVar coding SNVs, highly conserved)AUPRC (zero-shot; ClinVar coding SNVs, moderately conserved)AUPRC (zero-shot; ClinVar coding SNVs, near splice site)AUPRC (zero-shot; ClinVar coding SNVs, not conserved)AUPRC (zero-shot; ClinVar coding SNVs, poorly conserved)AUPRC (zero-shot; ClinVar coding SNVs)AUROC (zero-shot; ClinVar coding indels)AUROC (zero-shot; ClinVar coding microsatellite variants)AUROC (zero-shot; ClinVar coding non-SNVs, far from splice site)AUROC (zero-shot; ClinVar coding non-SNVs, highly conserved)AUROC (zero-shot; ClinVar coding non-SNVs, moderately conserved)AUROC (zero-shot; ClinVar coding non-SNVs, not conserved)AUROC (zero-shot; ClinVar coding non-SNVs, poorly conserved)AUROC (zero-shot; ClinVar coding SNVs, far from splice site)AUROC (zero-shot; ClinVar coding SNVs, highly conserved)AUROC (zero-shot; ClinVar coding SNVs, moderately conserved)AUROC (zero-shot; ClinVar coding SNVs, near splice site)AUROC (zero-shot; ClinVar coding SNVs, not conserved)AUROC (zero-shot; ClinVar coding SNVs, poorly conserved)AUROC (zero-shot; ClinVar coding SNVs)
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding indels classification (Evo 2 paper, Supplementary Data 1)0.931Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.809Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding microsatellite variants classification (Evo 2 paper, Supplementary Data 1)Not reported0.692Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.814Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reported0.92Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.808Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reported0.986Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.832Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding non-SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reported0.897Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.736Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding non-SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reported0.713Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.512Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding non-SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reported0.772Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.654Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.957Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.923
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.957Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.926Not reportedNot reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.967Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.889Not reportedNot reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.856Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.903Not reportedNot reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, near splice site classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.966Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.895Not reportedNot reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.802Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.899Not reportedNot reported
ESM-1b (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar coding SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.853Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.937Not reported
All 28 result rows with coverage, uncertainty and sources
Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding indels classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.931 AUPRC (zero-shot; ClinVar coding indels)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding indels (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-indel

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J66, row 66: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'Indel', Sub_category '', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding indels classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.809 AUROC (zero-shot; ClinVar coding indels)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding indels (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-indel

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I66, row 66: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'Indel', Sub_category '', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding microsatellite variants classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.692 AUPRC (zero-shot; ClinVar coding microsatellite variants)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding microsatellite variants (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-microsatellite

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J94, row 94: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'Microsatellite', Sub_category '', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding microsatellite variants classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.814 AUROC (zero-shot; ClinVar coding microsatellite variants)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding microsatellite variants (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-microsatellite

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I94, row 94: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'Microsatellite', Sub_category '', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.92 AUPRC (zero-shot; ClinVar coding non-SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J156, row 156: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Far from splice site', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.808 AUROC (zero-shot; ClinVar coding non-SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I156, row 156: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Far from splice site', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.986 AUPRC (zero-shot; ClinVar coding non-SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J339, row 339: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Highly conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.832 AUROC (zero-shot; ClinVar coding non-SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I339, row 339: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Highly conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.897 AUPRC (zero-shot; ClinVar coding non-SNVs, moderately conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, moderately conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-moderately-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J283, row 283: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Moderately conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.736 AUROC (zero-shot; ClinVar coding non-SNVs, moderately conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, moderately conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-moderately-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I283, row 283: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Moderately conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.713 AUPRC (zero-shot; ClinVar coding non-SNVs, not conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, not conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-not-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J412, row 412: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Not conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.512 AUROC (zero-shot; ClinVar coding non-SNVs, not conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, not conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-not-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I412, row 412: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Not conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.772 AUPRC (zero-shot; ClinVar coding non-SNVs, poorly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, poorly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-poorly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J464, row 464: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Poorly conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding non-SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.654 AUROC (zero-shot; ClinVar coding non-SNVs, poorly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding non-SNVs, poorly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-non-snv-poorly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I464, row 464: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'non-SNV', Sub_category 'Poorly conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.957 AUPRC (zero-shot; ClinVar coding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J4, row 4: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.923 AUROC (zero-shot; ClinVar coding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I4, row 4: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.957 AUPRC (zero-shot; ClinVar coding SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J117, row 117: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Far from splice site', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.926 AUROC (zero-shot; ClinVar coding SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I117, row 117: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Far from splice site', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.967 AUPRC (zero-shot; ClinVar coding SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J306, row 306: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Highly conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.889 AUROC (zero-shot; ClinVar coding SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I306, row 306: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Highly conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.856 AUPRC (zero-shot; ClinVar coding SNVs, moderately conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, moderately conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-moderately-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J247, row 247: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Moderately conserved', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.903 AUROC (zero-shot; ClinVar coding SNVs, moderately conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, moderately conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-moderately-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I247, row 247: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Moderately conserved', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, near splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.966 AUPRC (zero-shot; ClinVar coding SNVs, near splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, near splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-near-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J137, row 137: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Near splice site', column 'AUPRC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, near splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.895 AUROC (zero-shot; ClinVar coding SNVs, near splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, near splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-near-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I137, row 137: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Near splice site', column 'AUROC'
Configuration: ESM-1b (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar coding SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.802 AUPRC (zero-shot; ClinVar coding SNVs, not conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

ESM-1b on ClinVar coding SNVs, not conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-coding-snv-not-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J367, row 367: Model 'ESM-1b', Data 'ClinVar', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category 'Not conserved', column 'AUPRC'

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Stable ID: gfm-guides-20261014-evo2-brixi2026-config-esm-1b

areas
dna-genomes
contexts
research
method types
foundation_model
reported name
ESM-1b
foundation model eligible
true
parameters
Protein language model (reference 127)
source locator
Supplementary Data 1 column 'Model' ('ESM-1b'); SI A.3.12 (page 13)
version
ESM-1b
missing metadata
access reuse: reason: unextracted; checkpoint revision: reason: unreported
provenance note
ESM-1b as scored zero-shot by the Evo 2 authors on human variant effect benchmarks.
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